Development of chiral metal amides as highly reactive catalysts for asymmetric [3 + 2] cycloadditions
Highly efficient catalytic asymmetric [3 + 2] cycloadditions using a chiral copper amide are reported. Compared with the chiral CuOTf/Et3N system, the CuHMDS system showed higher reactivity, and the desired reactions proceeded in high yields and high selectivities with catalyst loadings as low as 0....
Main Authors: | Yasuhiro Yamashita, Susumu Yoshimoto, Mark J. Dutton, Shū Kobayashi |
---|---|
Format: | Article |
Language: | English |
Published: |
Beilstein-Institut
2016-07-01
|
Series: | Beilstein Journal of Organic Chemistry |
Subjects: | |
Online Access: | https://doi.org/10.3762/bjoc.12.140 |
Similar Items
-
Novel chiral phosphonium ionic liquids as solvents and catalysts for cycloadditions. Investigation of the Diels-Alder reaction of a series of dienes and dienophiles in novel chiral phosphonium ionic liquids.
by: Yu, Jianguo
Published: (2010) -
Cycloadditions of heterocyclic sulphinylamines
by: Wren, S. A. C.
Published: (1986) -
Chiral Bis(Imidazolidine)Pyridine-Cu Complex-Catalyzed Enantioselective [3+2]-Cycloaddition of Azomethine Imines with Propiolates
by: Yuta Ogino, et al.
Published: (2012-05-01) -
Silver-catalysed azide–alkyne cycloaddition (AgAAC): assessing the mechanism by density functional theory calculations
by: Biswadip Banerji, et al.
Published: (2016-01-01) -
Synthesis of chiral sulfoximine-based thioureas and their application in asymmetric organocatalysis
by: Marcus Frings, et al.
Published: (2012-09-01)